4.7 Article

Real-time red blood cell counting and osmolarity analysis using a photoacoustic-based microfluidic system

Journal

LAB ON A CHIP
Volume 21, Issue 13, Pages 2586-2593

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1lc00263e

Keywords

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Funding

  1. National Natural Science Foundation of China [61925307, 61727811, U1908215, 61973298]
  2. External Cooperation Program of the Chinese Academy of Sciences [173321KYSB20170015]
  3. CAS Interdisciplinary Innovation Team [JCTD-2019-09]
  4. Youth Innovation Promotion Association of the Chinese Academy of Sciences [Y201943]
  5. Hong Kong Research Grants Council [9042639, 907002, JLFS/E-104/18]

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The study explores the use of photoacoustic detection for characterizing RBCs, which is faster and less invasive compared to traditional methods. Compared to conventional microfluidic analysis methods using camera-captured image sequences, the photoacoustic method requires only processing one-dimensional time-series data, resulting in lower computational requirements.
Counting the number of red blood cells (RBCs) in blood samples is a common clinical diagnostic procedure, but conventional methods are unable to provide the size and other physical properties of RBCs at the same time. In this work, we explore photoacoustic (PA) detection as a rapid label-free and noninvasive analysis technique that can potentially be used for single RBC characterization based on their photoabsorption properties. We have demonstrated an on-chip PA flow cytometry system using a simple microfluidic chip combined with a PA imaging system to count and characterize up to similar to 60 RBCs per second. Compared with existing microfluidic-based RBC analysis methods, which typically use camera-captured image sequences to characterize cell morphology and deformation, the PA method discussed here requires only the processing of one-dimensional time-series data instead of two- or three-dimensional time-series data acquired by computer vision methods. Therefore, the PA method will have significantly lower computational requirements when large numbers of RBCs are to be analyzed. Moreover, we have demonstrated that the PA signals of RBCs flowing in a microfluidic device could be directly used to acquire the osmolarity conditions (in the range of 124 to 497 mOsm L-1) of the medium surrounding the RBCs. This finding suggests a potential extension of applicability to blood tests via PA-based biomedical detection.

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